STERILOX LIQUID CHEMICAL STERILANT SYSTEM

STERILOX LIQUID CHEMICAL STERILANT SYSTEM is an FDA 510(k)-cleared medical device (K063159) manufactured by Puricore, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 1, 2007. Regulation: 8.